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Pregnancy, Unwanted clinical trials

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NCT ID: NCT04830007 Suspended - Pregnancy, Unwanted Clinical Trials

Factors Associated With the Absence of Contraception at Women Seeking a Voluntary Termination of Pregnancy

Start date: November 2022
Phase:
Study type: Observational

The study will be offered to all women who are consultant for an abortion plan are seen in consultation at the orthogeny center where the study will be conducted. Of these 700 women, about 10% will not agree to participate in the study and 10% will not meet the inclusion criteria. Thus it's plane to include 560 patients in the study.

NCT ID: NCT03774745 Terminated - Pregnancy, Unwanted Clinical Trials

Blocking Mifepristone Action With Progesterone

Start date: February 11, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Double-blind randomized trial to evaluate the potential impact of progesterone treatment on early pregnancies exposed to mifepristone.

NCT ID: NCT03519191 Terminated - Violence Clinical Trials

Healthy Relationships and Economic Pathways

H-REP
Start date: June 1, 2017
Phase: N/A
Study type: Interventional

The California Adolescent Health Collaborative (CAHC) brings together multiple nonprofit organizations in California's Central Valley to implement the Healthy Relationships and Economic Pathways (H-REP) program, which aims to increase and promote healthy relationships and stability among youth between the ages of 14 and 24.

NCT ID: NCT02447029 Completed - Pregnancy, Unwanted Clinical Trials

Self-Administered Lidocaine Gel for Pain Management With First Trimester Surgical Abortion: A Randomized Controlled Trial

SALSA
Start date: April 2015
Phase: Phase 3
Study type: Interventional

Despite global efforts to decrease discomfort during surgical abortion, pain remains a limiting factor in where and how procedures are performed. Several studies have investigated different methods of delivering cervical anesthesia prior to abortion, however to the best of the investigators' knowledge, there is no published data that 1) rigorously examines the effect of a time interval between local anesthetic administration and procedure initiation, or 2) explores whether adequate pain relief is possible through self-administered, non-invasive means alone. Research in this area has a significant public health impact, given the large number of women worldwide who seek abortions. The investigators propose to explore the effect of a locally applied vaginal lidocaine gel in place of the traditional paracervical block prior to first trimester surgical abortion. They hypothesize that lidocaine gel is no worse than paracervical block at decreasing abortion related pain at a variety of time points throughout the procedure. This is a non-inferiority, open label, randomized controlled trial. If self-administered vaginal gel is acceptable and effective, it would increase options for pain control during abortion and other gynecologic procedures.